Cas 869767-83-9,1H-Benzimidazole-5-carboximidamide, N-hydroxy-2-[4-[6-[(hydroxyamino)iminomethyl]-3-pyridinyl]phenyl]-

869767-83-9

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Basic information

Product Name: 1H-Benzimidazole-5-carboximidamide, N-hydroxy-2-[4-[6-[(hydroxyamino)iminomethyl]-3-pyridinyl]phenyl]-
Synonyms:
CAS NO:869767-83-9
Molecular Formula: C20H17N7O2
Molecular Weight: 387.401
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1H-Benzimidazole-5-carboximidamide, N-hydroxy-2-[4-[6-[(hydroxyamino)iminomethyl]-3-pyridinyl]phenyl]-(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Benzimidazole-5-carboximidamide, N-hydroxy-2-[4-[6-[(hydroxyamino)iminomethyl]-3-pyridinyl]phenyl]-(869767-83-9)
EPA Substance Registry System: 1H-Benzimidazole-5-carboximidamide, N-hydroxy-2-[4-[6-[(hydroxyamino)iminomethyl]-3-pyridinyl]phenyl]-(869767-83-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 869767-83-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 869767-83-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,7,6 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 869767-83:
(8*8)+(7*6)+(6*9)+(5*7)+(4*6)+(3*7)+(2*8)+(1*3)=259
259 % 10 = 9
So 869767-83-9 is a valid CAS Registry Number.

869767-83-9Upstream product

869767-83-9Downstream Products

869767-83-9Relevant academic research and scientific papers

Dicationic near-linear biphenyl benzimidazole derivatives as DNA-targeted antiprotozoal agents

Ismail, Mohamed A.,Batista-Parra, Adalgisa,Miao, Yi,Wilson, W. David,Wenzler, Tanja,Brun, Reto,Boykin, David W.

, p. 6718 - 6726 (2007/10/03)

A series of near-linear biphenyl benzimidazole diamidines 5a-h were synthesized from their respective diamidoximes (4a-h), through the bis-O-acetoxyamidoxime, followed by hydrogenation in glacial acetic acid/ethanol in the presence of Pd-C. Compounds 4a-h

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